Methods and devices for in vivo repair of cardiac stimulator leads

• US 5,876,429 A
• Filed: 06/07/1995
• Issued: 03/02/1999
• Est. Priority Date: 06/07/1995
• Status: Expired due to Fees

• Current Assignee: Intermedics Incorporated (Boston Scientific Corporation)
• Original Assignee: Intermedics Incorporated (Boston Scientific Corporation)
• Inventors: Schroeppel, Edward A.
• Primary Examiner(s): Nasser, Robert L.
• Application Number:
  US08/472,518
• Time in Patent Office: 1,364 Days
• Field of Search: 128/642, 128/641, 128/898, 607/115, 607/116, 607/119, 607/122, 607/123, 607/132, 606/198, 623/1, 623/11, 623/12
• US Class Current: 607/115
• CPC Class Codes: A61N 1/057 Anchoring means; Means for fixing the head inside the heart
• CPC Class Codes: A61N 2001/0578 having means for removal or extraction
• CPC Class Codes: A61N 2001/0582 Suture sleeves

Abstract

The present invention provides devices and methods for using such devices which can be positioned over cardiac stimulator lead sections which are known to be flawed or which are at risk of failure, such as wire stiffener fractures and electrical shorts. The devices and methods of the invention can protect a patient with an implanted cardiac stimulator whose flawed lead represents a threat to his health or life. The devices and methods of use of the invention provide movable sleeves which can be positioned at various points along the length of a lead at the discretion of the heart surgeon.

Claims

1. A repair device adapted for attachment to an implantable cardiac stimulator lead situated within, or to be implanted into a person'"'"'s body, and being in need of repair or protection, said repair device comprising:

a hollow cylindrical sleeve comprising a metallic wire stent capable of assuming initially an expanded configuration and finally a relaxed configuration;

said sleeve having a predetermined length substantially less than that of a conventional cardiac stimulator lead, and in said relaxed configuration having an internal diameter substantially the same as an outer diameter of a conventional cardiac stimulator lead, said relaxed configuration being one in which, at body temperature, causes the greatest amount of compression of said sleeve;

whereby upon being positioned over a predetermined section of a lead in need of protection or repair, and upon assuming said relaxed configuration, said device effectuates repair or prevents damage to said lead.

2. The device of claim 1 wherein said device is biocompatible.

3. The device of claim 1 wherein said sleeve is capable of excluding substantially all fluids from said section of said lead.

4. The device of claim 1 wherein said stent is held in said expanded configuration by a water soluble coating.

5. The device of claim 4 wherein said water soluble coating is a gelatinous substance.

6. The device of claim 4 wherein said water soluble coating is a polysaccharide substance.

7. The device of claim 1 wherein said metallic wire stent comprises stainless steel.

8. The device of claim 1 wherein said metallic wire stent comprises a thermal-shaped memory alloy.

9. The device of claim 8 wherein said thermal-shaped memory alloy is nitinol.

10. The device of claim 1 wherein said metallic wire stent comprises tantalum.

11. The device of claim 1 wherein said sleeve further comprises on its outer surface a suture attachment structure.

12. The device of claim 1 wherein said sleeve further comprises on its inner surface a lead attachment structure capable of preventing dislodgement of said sleeve from said section of said lead.

13. The device of claim 12 wherein said lead attachment structure is a barb capable of penetrating surface insulation of said lead.

14. The device of claim 1 wherein said sleeve is sufficiently flexible to be threaded onto said lead proximal to connectors and suture attachment structures affixed to said lead and slidably passed over said connectors and suture attachment structures to assume a position distal to said connectors and suture attachment structures.

15. The device of claim 1 wherein the minimum diameter of said sleeve in said expanded configuration is large enough to allow said device to be slidably positioned over a predetermined section of a conventional implantable cardiac lead.

16. The device of claim 1 wherein said stent is helically-woven wire.

17. The device of claim 1 wherein said sleeve comprises means for expanding the diameter of said sleeve and means for reducing the diameter of said sleeve.

28. A method of repairing an implanted cardiac stimulator lead in situ, comprising:

threading the repair device of claim 1 onto a lead situated within a patient'"'"'s body, said lead being in need of repair or protection;

placing said device along said lead at a position proximal to a section of said lead subject to or experiencing a defect;

positioning said device over said section of said lead; and

affixing said device to said lead.

29. A method of protecting an implantable cardiac stimulator lead, comprising:

threading the repair device of claim 1 onto a lead, said device being adapted for being fitted onto said lead prior to or contemporaneously with implantation of said lead;

placing said device along said lead at a position proximal to a section of said lead subject to occurrence of a defect while implanted;

positioning said device over said section of said lead; and

affixing said device to said lead.

18. A repair device adapted for attachment to an implantable cardiac stimulator lead situated within a patient'"'"'s body, and having a flawed wire lead stiffener or defibrillation outer wire coil, said repair device comprising:

a hollow cylindrical sleeve comprising a metallic wire stent capable of assuming initially an expanded configuration and finally a relaxed configuration;

said sleeve having a predetermined length substantially less than that of a conventional cardiac stimulator lead, and in said relaxed configuration having an internal diameter substantially the same as an outer diameter of a conventional cardiac stimulator lead, said relaxed configuration being one in which, at body temperature, causes the greatest amount of compression of said sleeve;

whereby upon being positioned over a predetermined section of a lead in need of protection or repair, and upon assuming said relaxed configuration, said device effectuates repair or prevents damage to said lead.

19. A repair device adapted for attachment to an implantable cardiac stimulator lead situated within a patient'"'"'s body, and having a lead short, said repair device comprising:

a hollow cylindrical sleeve comprising a metallic wire stent capable of assuming initially an expanded configuration and finally a relaxed configuration;

said sleeve having a predetermined length substantially less than that of a conventional cardiac stimulator lead, and in said relaxed configuration having an internal diameter substantially the same as an outer diameter of a conventional cardiac stimulator lead, said relaxed configuration being one in which, at body temperature, causes the greatest amount of compression of said sleeve;

whereby upon being slidably positioned over a predetermined section of a lead in need of protection or repair, and upon assuming said relaxed configuration, said device effectuates repair or prevents damage to said lead.

20. A method of repairing an implantable cardiac stimulator lead, comprising:

constructing a hollow cylindrical sleeve;

said sleeve having a length substantially less than that of a lead situated within, or to be implanted into a patient'"'"'s body, said lead being in need of repair or protection;

said sleeve having an internal diameter substantially the same as an outer diameter of said lead;

threading said sleeve onto said lead;

placing said sleeve along said lead at a position proximal to a predetermined section of said lead subject to or experiencing a defect;

positioning said sleeve over said section of said lead and thereby effectuating repair of said lead or preventing further damage from a defect that may occur in said lead while said lead is in the patient'"'"'s body; and

,

affixing said sleeve to said lead.

21. The method of claim 20 wherein said positioning step is accomplished by slidably moving said sleeve along said lead length with a flexible tube slidably surrounding said lead proximal to said sleeve, said tube having an internal diameter less than an outer diameter of said sleeve but greater than said outer diameter of said lead.

22. The method of claim 21 wherein said tube is a coiled, flexible ribbon.

23. The method of claim 21 wherein said tube is a lead extractor sheath.

24. The method of claim 23 wherein said lead extractor sheath is a telescoping lead extractor sheath.

25. The method of claim 20 further comprising using said telescoping lead extractor sheath by:

fitting at a distal-most terminus of said sheath said sleeve in an expanded configuration;

telescoping said sheath along said lead to said section;

dislodging said sleeve from said distal-most terminus of said sheath to assume a contracted position on said lead at said section.

26. The method of claim 20 wherein said sleeve is placed along said lead by inserting said lead into an opening along said sleeve'"'"'s entire length, said opening having a width substantially the same or less than said outer diameter of said lead, said opening capable of allowing said sleeve to be fitted onto said lead at a position intermediate proximal and distal ends of said lead.

27. The method of claim 20 wherein said sleeve is lubricated prior to said positioning step in order to facilitate said positioning.